ENST00000375128.5:c.*35A>G
MANE Select
|
ENSP00000364270.5:n.*35A>G
|
|
ENST00000375128.4:c.*35A>G
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ENSP00000364270.4:n.*35A>G
|
|
ENST00000462523.5:c.*293A>G
|
ENSP00000433006.1:n.*293A>G
|
|
ENST00000485042.1:n.369A>G
|
|
|
NM_000380.3:c.*35A>G , LRG_471t1:c.*35A>G
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NP_000371.1:n.*35A>G
|
|
NR_027302.1:n.1205A>G
|
|
|
XM_006717278.1:c.772+85A>G
|
XP_006717341.1:n.772+85A>G
|
|
XM_011518988.1:c.772+85A>G
|
XP_011517290.1:n.772+85A>G
|
|
NM_001354975.1:c.*35A>G
|
NP_001341904.1:n.*35A>G
|
|
NR_149091.1:n.702A>G
|
|
|
NR_149092.1:n.868A>G
|
|
|
NR_149093.1:n.1394A>G
|
|
|
NR_149094.1:n.1288A>G
|
|
|
NM_000380.4:c.*35A>G
MANE Select
|
NP_000371.1:n.*35A>G
|
|
NM_001354975.2:c.*35A>G
|
NP_001341904.1:n.*35A>G
|
|
NR_027302.2:n.1136A>G
|
|
|
NR_149091.2:n.633A>G
|
|
|
NR_149092.2:n.799A>G
|
|
|
NR_149093.2:n.1325A>G
|
|
|
NR_149094.2:n.1219A>G
|
|
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